Canonical Allele Identifier: CA359719777
Gene: NDUFS4 HGNC NCBI

Linked Data

MyVariant Identifiers: chr5:g.52942176G>A (hg19) chr5:g.53646346G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.53646346G>A , CM000667.2:g.53646346G>A GRCh38
NC_000005.9:g.52942176G>A , CM000667.1:g.52942176G>A GRCh37
NC_000005.8:g.52977933G>A NCBI36
NG_008200.1:g.90712G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000296684.10:c.291G>A MANE Select ENSP00000296684.5:p.Trp97Ter
ENST00000296684.9:c.291G>A ENSP00000296684.5:p.Trp97Ter
ENST00000502423.5:c.*158G>A ENSP00000422177.1:n.*158G>A
ENST00000506765.1:c.279G>A ENSP00000424570.1:p.Trp93Ter
ENST00000506974.5:c.*67G>A ENSP00000425967.1:n.*67G>A
ENST00000507026.5:c.*265G>A ENSP00000424993.1:n.*265G>A
ENST00000509443.1:n.152G>A
NM_002495.2:c.291G>A NP_002486.1:p.Trp97Ter
XM_005248525.3:c.291G>A XP_005248582.1:p.Trp97Ter
XM_011543415.1:c.117G>A XP_011541717.1:p.Trp39Ter
NM_001318051.1:c.291G>A NP_001304980.1:p.Trp97Ter
NM_002495.3:c.291G>A NP_002486.1:p.Trp97Ter
NR_134473.1:n.493G>A
NR_134474.1:n.410G>A
NR_134475.1:n.445G>A
NM_002495.4:c.291G>A MANE Select NP_002486.1:p.Trp97Ter
NM_001318051.2:c.291G>A NP_001304980.1:p.Trp97Ter
NR_134473.2:n.487G>A
NR_134474.2:n.404G>A
NR_134475.2:n.439G>A
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